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Mid-level Validation Engineer

Katalyst Healthcares and Life Sciences
Decatur, IL Full Time
POSTED ON 3/1/2025
AVAILABLE BEFORE 5/26/2025

Responsibilities :

  • The manufacturing plant has new and existing manufacturing equipment / utilities that require validation.
  • 3-5 years of experience can be flexible.
  • Pharma / Bio Experience.
  • IQ,OQ,PQ Documents for Washers, autoclaves, isolators, clean utilities.
  • Validation Quality management system, drafting SOPS, drafting CAPA Change Control, Investigation.

Requirements :

  • Pharma / Biotech equipment validation : 3 years (Required).
  • Validation Quality management system : 3 years (Preferred).
  • Investigation : 3 years (Preferred).
  • Pharma / Bio : 3 years (Required).
  • IQ / OQ / PQ for Washers, autoclaves, isolators, clean utilities : 3 years (Required).
  • drafting CAPA change control : 3 years (Preferred).
  • drafting SOPs : 3 years (Preferred).

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